A Study Of Tocilizumab in Patients With Moderate to Severe Active Rheumatoid Arthritis Who Have an Inadequate Response to or Are Unable to Tolerate Biologic and Non-Biologic Disease-modifying Antirheumatic Drugs (DMARDs)

Completed · Phase 3

Conditions studied: Rheumatoid Arthritis

In brief

This 3 arm randomized open label study will evaluate the safety, tolerability and efficacy of tocilizumab in patients with moderate to severe active rheumatoid arthritis, who have had inadequate response to or are unable to tolerate DMARDs. The protocol incorporates risk mitigation strategies developed in partnership with the FDA to manage known and potential risks associated with the treatment of tocilizumab. Patients will be randomized to receive tocilizumab either 4 mg/kg intravenous (iv) or 8 mg/kg iv with concomitant non-biologic DMARDs, or 8 mg/kg iv without concomitant non-biologic DMARDs, every 4 weeks, for a total of 6 infusions. The anticipated time on study treatment is 3-12 months, and the target sample size is 500-1000 individuals.

Key facts

Study ID

NCT00891020

Run by

Hoffmann-La Roche

People needed

886

Starts

2009-05-01

Expected to finish

2011-03-01

Last updated by the study team

2012-10-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• adult patients, >=18 years of age;
• moderate to severe active rheumatoid arthritis for >6 months;
• inadequate clinical response or unable to tolerate current or prior biologic or non-biologic Disease-modifying antirheumatic drug (DMARD) therapy;
• Swollen joint count (SJC) >/=4 and Tender joint count (TJC) >/=4
• body weight </=150kg
• current permitted non-biologic DMARDs must be on stable dose for >/= 7 weeks prior to baseline;

You may not qualify if…

• history of autoimmune disease or inflammatory joint disease other than rheumatoid arthritis;
• functional class IV as defined by the American College of Rheumatology (ACR) Classification of Functional Status in rheumatoid arthritis;
• treatment with rituximab within 6 months before screening;
• intraarticular corticosteroids within 8 weeks or intramuscular (im)/ intravenous (iv) corticosteroids within 12 weeks prior to screening;
• known active current or history of recurrent infections, or any major episode of infection requiring hospitalization or treatment with iv antibiotics within 4 weeks of screening, or oral antibiotics within 2 weeks prior to screening.

Where it is running

• Study site — Birmingham, Alabama, United States
• Study site — Birmingham, Alabama, United States
• Study site — Huntsville, Alabama, United States
• Study site — Mobile, Alabama, United States
• Study site — Montgomery, Alabama, United States
• Study site — Tuscaloosa, Alabama, United States
• Study site — Hot Springs, Arizona, United States
• Study site — Paradise Valley, Arizona, United States
• Study site — Peoria, Arizona, United States
• Study site — Scottsdale, Arizona, United States
• Study site — Scottsdale, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Fayetteville, Arkansas, United States
• Study site — Fort Smith, Arkansas, United States
• Study site — Jonesboro, Arkansas, United States
• Study site — Little Rock, Arkansas, United States
• Study site — Covina, California, United States
• Study site — Escondido, California, United States
• Study site — Fullerton, California, United States
• Study site — Huntington Beach, California, United States
• Study site — La Jolla, California, United States
• Study site — Lakewood, California, United States
• Study site — Long Beach, California, United States
• Study site — Los Angeles, California, United States
• Study site — Anniston, Alabama, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.